@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP46806.RA80c4fFXhaiG-OL7lnfKNhwR1U8ETADYcessVnHWCR3k
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP46806.RA80c4fFXhaiG-OL7lnfKNhwR1U8ETADYcessVnHWCR3k130_head
{
this:
np:hasAssertion
dgn-np:NP46806.RA80c4fFXhaiG-OL7lnfKNhwR1U8ETADYcessVnHWCR3k130_assertion
;
np:hasProvenance
dgn-np:NP46806.RA80c4fFXhaiG-OL7lnfKNhwR1U8ETADYcessVnHWCR3k130_provenance
;
np:hasPublicationInfo
dgn-np:NP46806.RA80c4fFXhaiG-OL7lnfKNhwR1U8ETADYcessVnHWCR3k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP46806.RA80c4fFXhaiG-OL7lnfKNhwR1U8ETADYcessVnHWCR3k130_assertion
a
np:Assertion
.
dgn-np:NP46806.RA80c4fFXhaiG-OL7lnfKNhwR1U8ETADYcessVnHWCR3k130_provenance
a
np:Provenance
.
dgn-np:NP46806.RA80c4fFXhaiG-OL7lnfKNhwR1U8ETADYcessVnHWCR3k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP46806.RA80c4fFXhaiG-OL7lnfKNhwR1U8ETADYcessVnHWCR3k130_assertion
{
miriam-gene:11200
a
ncit:C16612
.
lld:C1527249
a
ncit:C7057
.
dgn-gda:DGNfc88d7727910f7755f771050fc8888c7
sio:SIO_000628
miriam-gene:11200
,
lld:C1527249
;
a
sio:SIO_001122
.
}
dgn-np:NP46806.RA80c4fFXhaiG-OL7lnfKNhwR1U8ETADYcessVnHWCR3k130_provenance
{
dgn-np:NP46806.RA80c4fFXhaiG-OL7lnfKNhwR1U8ETADYcessVnHWCR3k130_assertion
dcterms:description
"[The CHEK2 1100delC was not significantly increased in Swedish colorectal cancer patients, however, in order to determine the role of the variant in colorectal cancer families with the history of breast cancer a larger sample size is needed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:17214356
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP46806.RA80c4fFXhaiG-OL7lnfKNhwR1U8ETADYcessVnHWCR3k130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:21+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}